Genetics and Pediatric Unconjugated Hyperbilirubinemia
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference17 articles.
1. Evidence for a gene influencing serum bilirubin on chromosome 2q telomere: a genome-wide scan in the Framingham Study;Lin;Am J Hum Genet,2003
2. Genomic-wide association meta-analysis for total serum bilirubin levels;Johnson;Hum Mol Genet,2009
3. Risk factors for severe hyperbilirubinemia in neonates;Huang;Pediatr Res,2004
4. Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency: a dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia;Kaplan;Proc Natl Acad Sci USA,1997
5. Complex multifactorial nature of significant hyperbilirubinemia in neonates;Watchko;Pediatrics,2009
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1. Combined Effects of UGT1A1 and SLCO1B1 Variants on Chinese Adult Mild Unconjugated Hyperbilirubinemia;Frontiers in Genetics;2019-10-31
2. Hyperbilirubinemia and the Risk for Brain Injury;Neurology;2019
3. Gilbert syndrome in patients with type 1 diabetes-Prevalence, glycemic control, and microalbuminuria;Pediatric Diabetes;2017-01-17
4. Hereditary Contribution to Neonatal Hyperbilirubinemia;Fetal and Neonatal Physiology;2017
5. A Hypothesis for Using Pathway Genetic Load Analysis for Understanding Complex Outcomes in Bilirubin Encephalopathy;Frontiers in Neuroscience;2016-08-18
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